Why consider Novartis?
766 million. That’s how many lives our products touched in 2021. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives?We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges.
Imagine what you could do at Novartis!
Full-time interns are preferred but part-time arrangements are available for discussion!
Job Purpose
The Internship program focus on providing students with practical experience across RA functions. The intern would play a role in supporting regulatory activities for Novartis products. _________________________________________________________________________________
Major Accountabilities
- Support the RA team in preparing dossier packages for post-approval variations such as Chemistry Manufacturing and Control variations, change in artwork and other post-approval variations for registered products
- Support the RA team in preparing submissions for special consignment applications
- Any other RA activities as assigned by the management.
_________________________________________________________________________________
Ideal Background
- Currently enrolled in an accredited local University, preferably majoring in a science related major
- Demonstrate high level of interest and willingness to learn in Regulatory Affairs
- Good interpersonal, organizational, and communication skills
- Good command on healthcare and pharmacology terminology
- Computer literacy with knowledge of MS Office applications
____________________________________________________________________________
Personal Attributes
- Ability to work independently and in a team.
- Able to work within a multidisciplinary and multi-culturally team environment and independently as individual contributor.
- Able to share concepts, ideas, information and suggestions with peers.
- Able to manage multiple assignments and tasks, within tight timelines.
Reports to: Regulatory Affairs Manager/Associate Regulatory Affairs Manager
Related Job Searches:
- Company:
Novartis (Singapore) Pte Ltd - Designation:
Regulatory Affairs (RA) Intern - Profession:
Healthcare / Pharmaceutical / Sports - Industry:
Manufacturing General / Biomedical / Pharmaceutical - Location:
Queenstown